From studying autopsies of babies that were stillborn from infection, Dr. Andrew Moulden realized another process was happening concurrently: When the immune system is provoked, white blood cells (WBCs) migrate to capillaries that act as access roads to areas of need.

Ordinarily, WBCs squeeze through temporary cracks in vessel walls to fight nearby threats. But white blood cells are about twice as big as red blood cells, so when huge numbers of WBCs are released into circulation, they block blood flow through the microcirculation – particularly when sludging of RBCs is already elevated. Dr. Moulden called this scenario “Moulden Anoxia Spectra Syndrome” (MASS).

Plasma has the easiest time moving through vessels (slide A), movement of red blood cells is more restricted (B), and white blood cells have the hardest time getting all the way to where they are needed (C). In fact, they typically need to go “off-roading” to reach their destination.

White blood cells block the “side streets” of circulation

For context, red blood cells are larger than the smallest capillaries, so they have to contort themselves to fit through. To exchange gases, RBCs must be firm but flexible to brush up against vessel walls, drop off the oxygen they are carrying, and pickup carbon dioxide for removal. On the other hand, white blood cells are twice the diameter of red blood cells. To fight disorder, WBCs must have the ability to become formless, like an amoeba, to squeeze through temporary gaps in vessel walls.

Under normal circumstances, white blood cells travel through vessels just like any other type of cell: with a “laminar” (straight) flow and minimal friction. But when the immune system is called into action by pathogens, toxins or injury – perhaps due to loss of e-zone along vessel walls – finger-like projections raise up from the vessel walls, creating a bristly surface. Their counterpart, WBCs, have the consistency of a squishy bean bag with a rough outer surface of their own.

In this state of immune system activation, WBCs rub against vessel walls, they: (1) roll like a snowball, (2) adhere to the vessel wall at an area of need, and (3) then squeeze through gaps in the wall to begin healing local tissues. It’s the positive charge of damaged tissue that attracts WBCs where they are needed. This describes the normal signaling and healing process of immune cells.

How Moulden Anoxia Spectra Syndrome starts

When the immune system is activated, red blood cells whiz by at full (laminar) speed. But WBCs rely on water pressure to roll them like a tumbleweed, instead of pushing them directly from behind. Point being, only a fraction of the total blood pressure and momentum produces forward motion for WBCs. Therefore, when the blood loses momentum, WBCs are the first blood product to slow down or stop.

Hence, their rolling action and large size make white blood cells cause more clots, more easily – especially when blood is sludgy and the system is flooded with them. In short, when the immune system releases masses of WBCs – whatever the reason – blood flow is obstructed into, and out of, that area of engagement. Circulation through those areas then comes to a virtual standstill, especially through the smallest vessels. This begins the MASS activation process.

This is where the concept of vaccination runs into real-world complications. You see, by flooding an already (1) zeta-compromised system with: (2) pathogenic agents such as spike proteins, (3) white blood cells, and (4) adjuvants such as aluminum, you make people more vulnerable to deficiency or outright injury from lack of circulation.

Moreover, aluminum has traditionally been the vaccine ingredient most responsible for causing neurological disorders and autoimmune reactions in (mostly) children (although mRNA spike proteins will certainly surpass aluminum in net damage done). Autoimmunity is a big deal because it’s traditionally been the most destructive, long-term complication of vaccination.

Dr. Andrew Moulden: “When the non-specific (innate) immune system is in this state of “hypervigilance,” any concurrent immune challenge (e.g., gluten, casein, lactose – if intolerant, febrile illness, infection, antibiotic use…) will aggravate the underlying MASS response pathophysiology and lead to greater discomfort, disease, and clinical symptoms for the patient.”

How aluminum collects in areas

Western medicine has long operated on the assumption that aluminum disperses evenly throughout the body and deconcentrates as it is eliminated. Whether aluminum is ingested or injected, drug companies and public health agencies basically say, “Don’t worry about how much aluminum we’re putting in vaccines. Even though it’s extremely toxic, detox organs can get rid of it before it harms you.” This is a disastrous theory/lie.

The truth is, immune cells do identify aluminum as a toxin. When they encounter aluminum, white blood cells gobble it up and hold it in their anatomy, where it can’t hurt our cells and tissues. Unfortunately, they don’t take aluminum to a detox organ to harmlessly dispose of it. Instead, aluminum can’t be rendered non-toxic, so it rides around inside the white cell while it goes about its business. Like a Trojan Horse scenario, this gives aluminum access to secured areas, such as brain tissue behind the blood-brain barrier.

Unfortunately for us, when the immune system calls these aluminum-bearing WBCs to an area, and they expire from clotting, combat or old age, they drop their aluminum on the spot, while dead cell fragments get recycled. This is how aluminum and other heavy metals collect in areas needing restoration. Aluminum is brought to an area in response to infection, injury, hyperactivation (of a brain center, for example), inflammation, toxicity or even false signaling.

When a WBC carrying the aluminum does not leave for whatever reason, that area becomes a toxic waste dump. Even worse, these potent neurotoxins accumulate in the most damaging places possible: in the fatty tissues of the brainstem, heart, endocrine organs or nervous system. This is part 2 of the Moulden Anoxia Spectra Syndrome process.

How bacteria hijack white blood cells

When exposed to antibiotics or aluminum, some kinds of bacteria have the unusual ability to lose their cell walls without perishing. Indeed, this is the method by which antibiotics operate: They prevent bacteria from building/repairing cell walls. Aluminum is thought to do the same thing. Normally, when exposed to an antibiotic, a bacterium will simply burst. If it can’t repair its cell wall, its innards will spill out, and most will die. However, some strains have the ability to enter a white blood cell, replicate, take over the cell, and then evade detection by our immune system.

As you can imagine, hiding inside WBCs both decreases the immune system’s number of productive cells and, at the same time, increases the scope and duration of the fight. Unfortunately, the immune system has a hard time detecting which cells have been compromised by intracellular bacteria, so it just makes more white cells, hoping some will stay viable. That is, some WBCs may be fighting with you (on your side), while others may sabotage your immune system’s best efforts (having been hijacked). This double-whammy insult to WBC function weakens and confuses a person’s immune response.

When combined with the preceding Trojan Horse scenario (very common), you get hot spots of inflammation in the brain, kidneys, digestive tract, thyroid, skin or other organs/tissues that cause chronic, degenerative conditions. To make matters worse, the greater the distress signal to an organ or tissue, the more aluminum and pathogens are brought there, thereby keeping the inflammatory cascade going unless/until the immune system can get ahead of the pathology process. As a result, inflammation can smolder along for years or decades, until a bit hit like a major infection or toxin exposure tips the inflammatory cascade in the wrong direction.

This scenario could be, and probably is, the way that antibiotics and aluminum prolong bacterial (and possibly viral) infections in those that get sick easily and can’t recover: they’re harboring low-grade infections in isolated areas that transport heavy metals to disaster areas.

We already know that aluminum is used as an adjuvant to intensify (protract) the immune response. So now we can say with reasonable certainty that aluminum either helps pathogens evade detection, and/or it antagonizes the immune system as if the pathogen were wielding aluminum as its own pro-inflammatory, neurotoxic weapon.

On a side note, this process of endosymbiosis (two life forms uniting) suggests how mitochondria (thought to have evolved from bacteria) may have come to inhabit eukaryotic (e.g., human) cells millions of years ago. Ancient archaea (primitive bacteria) and bacteria hooked up by chance encounter such as this, and found the partnership mutually beneficial, so they kept it up.

Moulden Anoxia Spectra Syndrome (MASS), in Dr. Andrew Moulden’s own words

This entire section is a quote from an interview, with slight modifications for clarity. Descriptions in brackets are mine.

“Ischemic tissue [inadequate blood supply] attracts macrophages [type of white blood cell that engulf pathogens] that attempt to “clean up” the damaged tissue as well as the sedimented aluminum. This causes an inflammatory response (or not). The aluminum cannot readily be removed from the tissue since its large positive charge derails the negative electrostatic carrying capacity of the blood where the aluminum has accumulated. The blood vessels, muscle, and fascia in the tissue area will be damaged from the on-going ischemia and the inability to remove aluminum from the area (an electrical charge problem).

The macrophages and white blood cells will be called to this area to “clean up.” It is the act of the immune system chronically coming to this tissue area that perpetuate the problem and creates greater disease and the possibility for induction of an autoimmune response, or immunological tolerance through anergy [absence of immune response] or deletion.

Remarkably, the immune response, in biomechanics, causes further tissue damages, in some instances, from macrophagic myofaciitis to Type 1 diabetes to Parkinson’s disease to multiple sclerosis to Guillain-Barré syndrome to febrile seizures to autism spectrum to Crohn’s-colitis to sudden infant death – you name it.

Importantly, the vaccines are causing the exact same pathological sequence as wild polio virus does and did to cause paralysis and respiratory failure. This is the same mechanism by which:

• Thalidomide caused babies to be born with no arms and legs.
• Vioxx caused heart attack and stroke.
• Cholesterol lowering drugs are causing myalgia and mysositis.
• Spanish Flu killed 20 million in 1918.
• Swine flu vaccine caused paralysis.
• Hepatitis A/B vaccines are causing multiple sclerosis.
• A series of anthrax vaccines caused female vets to give birth to infants with no arms or legs 18 months after vaccination.
• All vaccines are causing autism spectrum and learning disabilities, SIDS and ADHD.
• Repeated flu vaccination causes dementia.
• Tetanus causes lockjaw, this is ischemic stroke, in evolution, to the brain from blocked blood flow.
• Vaccination induces Guillain-Barré syndrome (these are end vascular strokes, to descending motor tracts in the brain – brain damage).
• Smallpox killed and caused skin lesion. Each “pock” is caused by ischemia because germs colonize in places immune cells can’t go.
• Congenital rubella, in the pre-vaccine era, caused ischemic damages to brain body and lung.”

This US serviceman suffered the effects of “Gulf War Syndrome” after taking the anthrax vaccine. What impresses me most about his before-and-after pictures is how robust and strapping he looks before vaccination, and how affected and vulnerable he looks after being vaccinated. He looks like a completely different person. Indeed, he can’t look at himself in a mirror now after realizing what was done to him.

The concepts developed by Moulden and Riddick explain why vaccines are harmful

• All vaccines cause some level of MASS and zeta pathology because every one of them assaults the immune system in order to “work.” Thus, if any vaccine, now or in the future, contains the following ingredients, it can never be made completely safe: (1) antigens (“antibody generator,” such as viral or bacterial agents), (2) adjuvants (immune system stimulants), (3) preservatives, and (4) contaminants such as foreign animal proteins or aborted fetal cells. In other words, the odds of injury from vaccination may be exactly the opposite of what you think. So instead of a low single-digit chance that your child will be seriously injured by a vaccine, a large majority (meaning most people) will suffer long-term immune hypervigilance, residual heavy metal toxicity, and compromised circulation from vaccination. We just couldn’t read the less-obvious signs of chronic injury, including nerve paralysis from microstrokes, so we assumed that children were completely unaffected.
• Vaccine damage is cumulative with each dose. Medical science has failed to recognize that microcirculation progressively worsens the more vaccines you take over time. And when sludging overwhelms your system, clots that often go unnoticed can turn into brain, organ, and/or autoimmune damage.
• Vaccines can affect people in many different ways and degrees – confusing practitioners as to both cause and effect.
• Multiple shots in one office visit multiplies coagulation, blood clots and nerve damage.
• Vaccines cause most of the same adverse effects as the infection/germ itself because pathogens and vaccines share common mechanisms of injury: zeta collapse, poor blood flow and MASS. For instance, wild polio does similar damage to that of its vaccine (reasons mentioned above). Think of it this way: Drug companies weaken a virus and inject it into people in attenuated form. The antigen, all by itself, produces an immune response far too weak to confer immunity, so drug makers must add adjuvants to amplify the immune system’s reaction. In fact, it’s actually the body’s own healing response that does most of the damage when you’re fighting an infection, not the germs themselves. That means you feel sick because of measures the body takes to fight pathogens and toxins. The end result being, much of the injury reduction from attenuating a virus is replaced with adjuvants, preservatives and contaminants, thereby bringing the threat and injury back up.
• To top off the topic, the Substack author, A Midwestern Doctor, has lost count of the number of patients, colleagues and friends that have developed microclotting, partial paralysis of cranial nerves, and eye mis-alignment since getting the C19 shots – although they may not have known they were harmed, until it’s pointed out to them.

Mature adults can develop autistic features from vaccination in rare cases.

More factors affecting blood flow

I always wondered what caused tingling in my toes after eating lots of sugar

For decades, I wondered what caused that tingling sensation in my toes after eating very sugary food such as cookies or doughnuts. However, it doesn’t happen after I exercise, and/or in hot weather. Now I know why: High blood-sugar causes red blood cells to lose their negative charge. Having lost their slipperiness, they then stick to each other and clog up the smallest capillaries, particularly in the extremities. Therefore, tingling in the toes is a very good indication that nerves have fallen asleep from lack of oxygen.

This would also explain why I didn’t get this effect when drinking a sugary beverage after exercising: Aerobic exercise and hot weather dilate the blood vessels with nitric oxide, which offsets the lost in zeta potential. This phenomenon has huge implications for diabetics. It means sugar, which diabetics have difficulty getting into cells, decreases zeta potential on red blood cells. This makes them sticky, which thickens the blood. Lack of circulation through the extremities starves and eventually kills the nerves, which then causes neuropathic pain.

So, once again, medical science is half true, half incomplete, in its analysis. It isn’t sugar itself that damages nerves, causing neuropathy. Instead, sugar reduces zeta potential on RBCs, and thus capillary blood flow through the toes. This would explain why therapies such as red and infrared light therapy, neuromuscular electrical stimulation, and even warm foot baths have been known to restore circulation and alleviate neuropathic pain in diabetics. Western medicine blames sugar, when it’s more accurate to say a loss of electrical charge on blood cells clogs the small vessels and makes nerves misfire.

Standard treatment for high blood-sugar in hospital

When patients are treated in a hospital for ketoacidosis (excess sugars and acidic ketones from lack of insulin), standard practice is to give insulin, potassium and saline. Insulin drives sugar into cells aboard the saline solution and potassium follows. This is how mainstream medicine treats diabetics with dangerously-high blood-sugar level.

Although the combination is given primarily to reduce blood-sugar level and relieve dehydration, an unintended benefit may be in the cocktail’s ability to restore colloidal stability and blood flow. Acidic ketones exacerbate circulation problems because sugar/acidity/positive charge (they coincide) weakens zeta potential, while alkalinity (negative charge) supports it. So, after the threat of coma or death from high blood-sugar is dealt with, blood flow itself becomes the priority concern, whether sought by medical professionals or not.

Saline’s effect on the blood

A majority of the time, saline solution modestly enhances zeta potential because a 0.9% solution moves the salt concentration of your blood toward the middle. Whereas, giving water or salt alone may help or it may hurt. For this reason, the routine use of saline (and other solutions) explains many of the benefits that patients receive (unwittingly) from hospital care. However, it is important to note the effect that salt has on zeta potential follows a U-shaped curve (see below), so it depends on where your level starts out, and where you end up after administration.

Image source (above): “Control of Colloid Stability through Zeta Potential” by Thomas M. Riddick.

This is the real reason Western medicine demonizes sodium chloride: we get a lot in processed foods so, more often than not, it promotes coagulation. At high concentrations, the body responds by raising blood pressure and heart rate to compensate, which usually aggravate heart problems.

But, note to self: Medical “experts” are focused on the wrong thing. They’re trying to solve the wrong problem. You see, they demonize salt itself, when there are at least four other factors that are more on point: sodium-potassium ratio, sodium-water concentration, the processing of foods itself, and the U-shaped curve that mineral salts follow. See Part VII: Circulation Solutions of the series for more information.

On the flip side, if you’re low to begin with, salt helps blood flow. In fact, any electrolyte such as potassium chloride, sodium sulfate or potassium sulfate affects colloids in a similar manner: Each thickens the blood at low concentrations, thins the blood at medium concentrations, and progressively thickens at high to extremely-high concentrations. Thus, if your cardiologist recommends you go on a low-salt diet, you can either do that to reduce electrolyte concentration, and/or you may increase your level of hydration to dilute your level from the other side of that equation.

What’s happening at high electrolyte concentrations is that there are so many like-charge ions in the “bulk” solution trying to distance themselves from each another that they compress the double-layer of ions surrounding each particle, thereby bringing particles closer together.

The purpose of fever

Medical experts say the purpose of a fever when you’re sick is to activate the immune system and help it fight off infection. They say viruses and bacteria can’t stand the heat. But my new theory is, the immune system may raise body temperature when it’s fighting illness in order to offset the loss in circulation. I submit that circulation enhancement is a primary purpose of fever.

You see, whenever the immune system is hyperactivated, extra white blood cells and positive charge from the healing response stymie zeta potential and clog smaller vessels. So, to keep the blood flowing, the immune system dilates blood vessels with heat. Hence, your head pounds and your whole body throbs at the peak of illness, when your immune system is fully deployed. On the other hand, the fever and inflammation produced by vaccination usually doesn’t come close to the “sickness” of a natural disease process.

Consequently, this ischemic-injury protection is an unsung reason why the natural healing response from a wild-type infection offers fewer complications and better immunity post recovery, compared to vaccine-based “immunity.” To simplify that even more, real illness has circulatory safeguards that vaccines don’t reliably give you. So these vaccine “shortcuts” can and do cause circulation-related injuries that few have recognized until pioneers like Dr. Moulden came along.

Why can’t you get two infections at once and get twice as sick?

I always wondered why it seemed like you couldn’t get two infections/illnesses at the same time. Now I know why: It’s because the immune system’s response to any pathogen is largely the same. It calls the same immune cells into action, no matter what pathogen(s) may be present. And it launches pretty much identical oxidative/inflammatory processes.

Therefore, the quantity of infections you have, or even which variants, is not as important as the net immunological load. Whether you’re infected with one virus, two viruses, or one virus and one bacteria strain, the body’s response is substantially similar. Said differently, that icky feeling you get when you’re sick is your immune system’s inflammatory response, not primarily any damage that germs are doing.

Risk factors for poor blood flow

• deficiency of antithrombin III or proteins C and S (anticoagulant proteins made by the liver)
• kidney or liver dysfunction
• dehydration, toxins in water
• diabetes
• obesity
• sedentary lifestyle, staying stationary for long periods (e.g., long flights)
• slow detoxifier of heavy metals
• race
• age.

Zeta bandits

• vaccines
• aluminum, mercury and other heavy metals
• non-native EMF exposure
• blue light from smartphones, LED TVs, and LED lights
• sugar, carbs, acidic, processed foods in general
• hormonal birth control pills
• cigarettes, alcohol
• emotional stress, negative though patterns
• acute infections
  • polio
  • Guillain-Barré
  • smallpox
  • measles
  • mumps
  • rubella
  • tetanus.

Conclusion: Whenever the immune system is activated by an external threat, positive charge depletes your zeta potential, and white blood cells contribute to capillary clogging. As an example, seasonal allergens such as tree and grass pollen release histamine in allergy sufferers, which trigger a cascade of effects. Moderate histamine attacks might be felt mostly in the eyes, nose and throat, while severe reactions cause fever and inflammation throughout your whole body.

The take away: Histamine’s positive charge promotes sludging/clotting by lowering zeta and raising MASS. As part of the natural healing response, Nature reduced the potential for injury by programming histamine to vasodilate vessels (e.g., bloodshot eyes) so immune cells can get to areas of need.

Again, positive charge is the polarity of injury and imbalance in the body, so most threats activate the healing response with their positive charge. That’s why a long list of threats impair blood flow and all it enables. That means all infections, all vaccines, and all heavy metals such as aluminum impair circulation. If an exposure is harmful or foreign to the body, it’s bound to be positively charged and compromising to circulation.

Non-native electromagnetic frequencies (nnEMFs)

Microwave radiation is a major threat to the blood’s electro-chemistry. Non-native electromagnetic frequencies (nnEMFs) from cell phones, Wi-Fi and smart devices are among the most harmful exposures modern humans encounter daily because they collapse zeta potential, deform red blood cells, and mess with their oxygen-carrying capacity.

Electrosmog, as nnEMFs are also called informally, disfigures RBCs – turning their cell walls rough and misshapen. In this decrepit state, they can’t carry oxygen efficiently, which inhibits mitochondrial function. RBCs then clump together in rouleaux formations (like stacks of coins) – clearly zeta-depleted – further spoiling circulation.

Microwaves also directly conflict with the frequencies at which respiratory proteins in the mitochondria oscillate, thus making more free radicals and less ATP. But, most alarming, is the speed at which all of this happens. Exposure to nnEMFs corrupts zeta potential, blood viscosity, and oxygen exchange of RBCs in mere minutes.

It is a striking effect that I’m surprised the human body can tolerate. Our physiology can compensate to some extent, but one thing is for certain: man-made frequencies, absolutely, positively, drain our health and healing capacity chronically.

Heavy metals from chemtrails (geoengineering, stratospheric aerosol injections)

Nano-particles of aluminum, barium, strontium, cadmium and other heavy metals are now being sprayed into our upper atmosphere. Their (claimed) purpose is to dim the sun, make it rain, prevent rain, or otherwise change the weather. For this reason, scientists call it “geoengineering” or “solar radiation management.”

Advocates write and talk about stratospheric aerosol injections as if they are mere proposals, to be considered in the future as possible solutions to climate change. However, observers currently see chemtrails in every continent and country of the world, several times per week. To my knowledge, there are no exceptions in location.

Whatever they want to call it, and whatever the reason, heavy metals are raining down on all of us. And their health effects are both sinister and scary, considering no one knows what to do about them or how to stop globalists from perpetrating them across the globe. Skeptics may deny the existence of chemtrails all they want, but their use is recorded in government and military documents, over 300 patents, international treaties, and forums such as the UN.

The technology has been proven in practice beyond any doubt. And you can see footage all over the Internet of plane nozzles cycling on and off with their high-altitude aerosol sprays. This proves to anyone with eyes and critical thinking still intact that chemtrails are done intentionally and are not incidental contrails.

Climate scientists in the system not only admit that geoengineering is being done at the present time, they’re publicly campaigning for more. In fact, they’re openly calling for more geoengineering in public conferences, articles and think tanks. World powers such as China even admitted to using weather modification technologies before the 2008 Olympics in Beijing.

What’s in these chemtrails: The nano particles in chemtrails exactly match those named in geoengineering patents. Their claimed purpose is to deflect sunlight. Composed primarily of aluminum, barium, cadmium and strontium (and things far more grotesque), these heavy metals accumulate in our fatty tissues such as the brain and heart. They’re now being found in Northern California ground and air samples at 50,000% higher than normal concentration.

Their effects: First, the particulates in aerosols disturb the lungs, causing asthma and allergies. Next, the toxins upset the GI tract with accumulations from the ground. As they circulate in the blood, they settle mostly in the brain and nervous system, fatty tissue and vital organs. To our detriment, heavy metals cause neurological damage such as Alzheimer’s, dementia, loss of motor skills, and dulling of the intellect. They contribute substantially to most modern diseases by interfering with biochemical, enzymatic, hormonal, nutritional and detoxification process.

I, myself, have recently (2019-) noticed I’ve been having trouble finding and articulating words, loss of physical coordination, less mental clarity, and respiratory weakness – all unusual for me, but exactly what you’d expect from increased intake of heavy metals.

Aluminum, in particular, is known to damage neural pathways (e.g., Alzheimer’s), contribute to neuro-muscular disorders (e.g., Parkinson’s), interfere with detoxification and immunity, make people complacent, and cause memory problems. Aluminum is also a fire accelerant. It’s causing forest fires around the globe to burn much hotter and faster than they ever have.

Get a thorough overview of geoengineering in Dane Wigington’s documentary, “The Dimming”. Website: geoengineeringwatch.org. Short summary of stratospheric aerosol injections – link to video.

Blue light

Bluish-white light from computer screens and LED lights fundamentally stimulates our biology. This “cool white” light on the eyes and skin (as opposed to warm, yellowish-white light from incandescent light bulbs) turns on the daytime portion of our circadian cycles, based on its color temperature (think brightness of color). The lighter the blue, the more stimulating it is.

How it’s supposed to be: Blue light in morning sun tells your pituitary/hormonal system it’s time to wake up. It’s time to get moving, use that brain of yours, and get things done. Serving as your internal pharmacy, the awakened pituitary coordinates the release of hormones and neurotransmitters that fuel mental and physical activity. Cortisol, dopamine, adrenaline, and sex hormones such as testosterone are called into action, along with everything related to the stress response.

Blue light basically turns on the chemistry in your body to help you make things happen. Unfortunately, modern humans are doing a great job of messing up their daily biorhythms by exposing themselves to too much blue in their technology, non-stop from morning to night. As a result, your system gets over-stimulated chronically, and you get depleted of biochemicals that run your brain and endocrine organs. Blue light basically revs up your adrenal engine constantly, without ever allowing it to rest and recharge.

By signaling for a virtually continuous release of biochemicals all waking hours, blue light keeps your cortisol level high (the stress hormone), which raises your blood-sugar level. Cortisol and the stress response also slows digestion, interferes with sleep, and lowers your immune system. As we’ve talked about, sugar actively depletes zeta potential, which increases coagulability of the blood.

The dysregulation that blue light causes to hormone/endocrine systems also promotes weight gain in the process of throwing your biochemicals out of balance (e.g., shortened attention span). It’s far more disruptive chronically than people realize because it’s so pervasive, yet subtle in its effects.

Conclusions

Many people live on the edge between good blood flow and bad

The body constantly monitors and manages zeta potential to keep the blood thin enough to flow, yet thick enough to clot when it needs to. So when sugar, spike proteins, microwave EMFs, aluminum, or any positive-charge substances get into the blood, sludging and clotting can happen immediately if it pushes you over the threshold. For biology, this means your blood can hang out just on the good side of this threshold most of the time, and some new insult to the system can throw zeta potential into the agglomeration zone.

To bring zeta back into balance, the body employs pH-balancing chemicals and anticoagulants to try and break up clumps and clots, when they happen. For example, D-dimer is a clot buster used to dissolve clots, and prothrombin is a coagulant used to increase clotting. I would suspect the body has a much easier time correcting natural zeta disruptions such as sugar, than it does unnatural exposures such as spike protein vaccines, because its playbook for dealing with foods and acidic conditions is built in, whereas aluminum is problematic.

As examples, a frontline mechanism by which the body controls electrolyte concentration, and thereby sludginess of the blood, is simply making you thirsty (or not). When you overexercise (lactic acid), you’re compelled to rest. When the blood gets too acidic, respiration increases (O₂ alkalizes, while CO₂ acidifies). A diabetic may get tingly toes unless/until enough insulin is produced to help sugar leave the bloodstream and/or the body’s blood-thinning measures take effect.

Finally, pH level of the blood is tightly regulated between 7.35 to 7.45. Because pH balance can’t deviate from this narrow range (or else you can slip into a coma), it merely sets the stage for zeta potential, like fine-tuning your norm, rather than a power tool by which the body makes large adjustments.

Bottom line, the body is programmed to deal with natural occurrences. But the unnatural threats are not so easy for the body to handle. The detox system is limited in its ability to get rid of heavy metals such as aluminum and mercury, while the immune system is flat-out assaulted by vaccine ingredients.

For modern humans, all of this means that most of us now live our lives with dangerously little safety margin with which to resist imbalance and fix dysfunction. We’ve already depleted our healing and rebalancing reserves with toxic food and environments, so exposure to the wrong injection, chronic infection, moldy environment, air pollutant, or agro-chemical can then push a person into a full-blown health crisis.

This mind-blowing information has caused me to rethink my understanding of what causes chronic disease

I used to think modern disease arises primarily from disconnecting from nature (i.e., light, water, magnetism, and daily/seasonal cycles of the body), chronic inflammation, poor diet, and low redox potential (lack of negative charge). While still my main mechanisms of action, I’ve had to make room at the top for this new common denominator of disorder: MASS reactions and poor blood flow from zeta potential deficiency.

Now that I know more about the causes and effects of poor zeta potential, there is no doubt that microstrokes initiate a great many conditions that stump modern medicine to this day. Even more persuasive, connecting the dots so precisely gives us clear prescriptions on how to solve so many issues involving poor circulation, oxygenation, mitochondrial energy, and toxin removal. Now we know with much greater clarity how to create optimal health on purpose.

I like to say that when you understand a complex life problem completely, it often ceases to exist. When you’ve learned the spiritual lesson you were meant to learn, it no longer serves any useful purpose in your life and simply disappears. For example, learning to trust yourself and advocate for your loved ones, instead of blindly believing supposed authority figures, is a lesson a lot of busy consumers need to learn these days.

On the other hand, when you operate on half-truths, misdirection, assumptions and lies – originating mostly from those that create problems so they can sell you the solutions – you end up with a medical system that has never cured a single modern lifestyle disease (nor would they ever want to).

If zeta potential and MASS reactions are kept well-regulated, does this mean you’ll be protected from vaccine injury?

It pains me greatly to say this but, yes, I do believe if you avoided the most prominent mechanisms of vaccine injury, which are impaired circulation and immune system hyperactivation, you might be spared from their primary mechanisms of injury. I wouldn’t recommend this course of action, but doing a bunch of things to raise your adaptive capacity through the roof will also elevate your threshold for which insults simply lower your “health bank account,” vs. which ones do you real damage.

Remember, vaccines are filled with other questionable ingredients that can cause a range of horrible side effects too numerous to mention here. But at least you’ll have some protection against the #1 and #2 causes of sudden death and persistent health problems: poor circulation and immune system dysregulation. That could mean you can take more vaccines if you absolutely must, while minimizing the imbalance and dysfunction that they cause you. In other words, the zeta protocols in Part VII are the best functional, proactive insurance measures you can take against vaccine injury or death, should you opt to go the vaccination route.

Bottom line: Blood flow should be your #1 health and healing concern. I would place it above diet or exercise as a science to study and apply intentionally in your daily life – simply because life revolves around blood flow. It is the common denominator through which health or sickness occurs.

As for vaccines, they impair blood flow in every single individual, after every single dose. They leave the immune system hyperactivated in most people for years to decades. And those are just the common side effects. We didn’t even talk about the more serious complications that make vaccines so controversial. For these reasons plus a whole lot more, vaccines are a dangerous game to play. This series can raise your insight and awareness on the science and solutions, but it can’t fix all the problems that vaccines might create. You’ve been warned.

Read Part 6.